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CTGGTGTGAAGGAACATGGCCCTGT[A/G]TCAGAGGTGGCGGTGTCTCCGGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 612805 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR6878 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MIR6878 - microRNA 6878 | ||||||
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There are no transcripts associated with this gene. |
TARS2 - threonyl-tRNA synthetase 2, mitochondrial (putative) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271895.1 | 61 | Missense Mutation | TAT,TGT | Y,C 4 | NP_001258824.1 | |
NM_001271896.1 | 61 | Missense Mutation | TAT,TGT | Y,C 4 | NP_001258825.1 | |
NM_025150.4 | 61 | Missense Mutation | TAT,TGT | Y,C 4 | NP_079426.2 | |
XM_006711555.1 | 61 | Missense Mutation | TAT,TGT | Y,C 4 | XP_006711618.1 | |
XM_006711556.1 | 61 | Missense Mutation | TAT,TGT | Y,C 4 | XP_006711619.1 | |
XM_017002394.1 | 61 | Missense Mutation | TAT,TGT | Y,C 4 | XP_016857883.1 | |
XM_017002395.1 | 61 | Missense Mutation | TAT,TGT | Y,C 4 | XP_016857884.1 |